A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655138



Internal ID18606733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80567970..80642525hg38UCSC Ensembl
Innerchr7:80197286..80271841hg19UCSC Ensembl
Innerchr7:80035222..80109777hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3874556
hg1974556
hg1874556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025144
Supporting Variants
Samples
Known GenesCD36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655138
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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